Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6		Leber hereditary optic neuropathy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6	LHON (3 genes) - VUB	Leber hereditary optic neuropathy	Centrum Medische Genetica - UZ Brussel VUB
Hyperparathyroidism (gene panel)	AIP, MEN1, CDKN1B, PRKAR1A, RET		Familial isolated hyperparathyroidism	Centre de Génétique Humaine - CHU Sart-Tilman
Pituitary adenoma (4 genes)	MEN1, AIP, CDKN1B, PRKAR1A	Pituitary adenoma (4 genes) - ULG	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 4, Carney complex	Centre de Génétique Humaine - CHU Sart-Tilman
Pituitary adenoma (5 genes)	AIP, CDKN1B, MEN1, RET, PRKAR1A	Pituitary adenoma (5 genes) - UCL	Familial isolated pituitary adenoma, Silent pituitary adenoma, Null pituitary adenoma, Prolactinoma, Pituitary gigantism, Acromegaly	Centre de Génétique Médicale UCL
Carney syndrome	PRKAR1A		Carney complex	Centre de Génétique Médicale UCL
Hyperekplexia (3 genes)	SLC6A5, GLRA1, GLRB	Hyperekplexia (3 genes) - ULG	Hereditary hyperekplexia	Centre de Génétique Humaine - CHU Sart-Tilman

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